Abemaciclib, a selective cdk4/6 inhibitor, restricts the growth of pediatric ependymomas

Muh Lii Liang, Chun-Han Chen, Yun-Ru Liu, Man Hsu Huang, Yu Chen Lin, Tai Tong Wong, Sey En Lin, Shing Shiung Chu, Yi Huei Ding, Tsung-Han Hsieh

Research output: Contribution to journalArticlepeer-review

9 Citations (Scopus)


Pediatric ependymomas are a type of malignant brain tumor that occurs in children. The overall 10-year survival rate has been reported as being 45–75%. Maximal safe surgical resection combined with adjuvant chemoradiation therapy is associated with the highest overall and progression-free survival rates. Despite aggressive treatment, one-third of ependymomas exhibit recurrence within 2 years of initial treatment. Therefore, this study aimed to find new agents to overcome chemoresistance and defer radiotherapy treatment since, in addition, radiation exposure may cause long-term side effects in the developing brains of young children. By using integrated bioinformatics and through experimental validation, we found that at least one of the genes CCND1 and CDK4 is overexpressed in ependymomas. The use of abemaciclib, a highly selective CDK4/6 inhibitor, effectively inhibited cell proliferation and reduced the expression of cell-cycle-related and DNA-repair-related gene expression via the suppression of RB phosphorylation, which was determined through RNA-seq and Western blot analyses. Furthermore, abemaciclib effectively induced cell death in vitro. The efficiency of abemaciclib was validated in vivo using subcutaneously implanted ependymoma tissues from patient-derived xenografts (PDXs) in mouse models. Treatment with abemaciclib showed encouraging results in preclinical pediatric ependymoma models and represents a potential therapeutic strategy for treating challenging tumors in children.

Original languageEnglish
Article number3597
Pages (from-to)1-17
Number of pages17
Issue number12
Publication statusPublished - Dec 2020


  • Abemaciclib
  • Patient-derived xenografts
  • Pediatric ependymomas

ASJC Scopus subject areas

  • Oncology
  • Cancer Research


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